Curran Timothy G, Zhang Yi, Ma Daniel J, Sarkaria Jann N, White Forest M
1] Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA [2] Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Thermo-Fisher Scientific, San Jose, California 95134, USA.
Nat Commun. 2015 Jan 12;6:5924. doi: 10.1038/ncomms6924.
Absolute quantification of protein expression and posttranslational modifications by mass spectrometry has been challenging due to a variety of factors, including the potentially large dynamic range of phosphorylation response. To address these issues, we have developed MARQUIS-Multiplex Absolute Regressed Quantification with Internal Standards-a novel mass spectrometry-based approach using a combination of isobaric tags and heavy-labelled standard peptides, to construct internal standard curves for peptides derived from key nodes in signal transduction networks. We applied MARQUIS to quantify phosphorylation dynamics within the EGFR network at multiple time points following stimulation with several ligands, enabling a quantitative comparison of EGFR phosphorylation sites and demonstrating that receptor phosphorylation is qualitatively similar but quantitatively distinct for each EGFR ligand tested. MARQUIS was also applied to quantify the effect of EGFR kinase inhibition on glioblastoma patient-derived xenografts. MARQUIS is a versatile method, broadly applicable and extendable to multiple mass spectrometric platforms.
由于多种因素,包括磷酸化反应可能具有的较大动态范围,通过质谱对蛋白质表达和翻译后修饰进行绝对定量一直具有挑战性。为了解决这些问题,我们开发了MARQUIS-多重内标绝对回归定量法,这是一种基于质谱的新型方法,它结合了等压标签和重标记标准肽,为信号转导网络中关键节点衍生的肽构建内标曲线。我们应用MARQUIS在几种配体刺激后的多个时间点定量EGFR网络内的磷酸化动力学,从而能够对EGFR磷酸化位点进行定量比较,并证明对于所测试的每种EGFR配体,受体磷酸化在性质上相似但在数量上不同。MARQUIS还被应用于定量EGFR激酶抑制对胶质母细胞瘤患者来源异种移植物的影响。MARQUIS是一种通用方法,广泛适用于多种质谱平台并且可扩展。